Living With Lupus

Write Yourself a Love Letter

With Valentine’s Day a few days away, I wanted to talk about love with my readers. The greatest love you’ll ever find that will help get you far in life

She's Got Lupus

Living With Lupus

February 10, 20210Comments

Mom Guilt & Chronic Illness

Being a parent is tough. Being a single mom to three boys is tougher. Now, being a single mom to three boys as a disabled chronically ill parent is extremely

by Rosadela Durruthy

She's Got Lupus

Living With Lupus

Lupus Pain

Lupus Warrior Spotlight

January 2, 20210Comments

My Lupus Warrior

My dad had one brother, Pedro Rolando Durruthy. Growing up I always heard stories from their youth in Cuba and moving to America. Them growing up in Boston, Massachusetts two

December 28, 20200Comments

Do I need to exercise?

Having lupus I have always struggled with wanting to exercise and not feeling up to it. Lately I've been lazy with my daily exercising routine and my body is reacting

by Rosadela Durruthy

She's Got Lupus

November 7, 20200Comments

Beginners Guide to Lupus

So you've just been diagnosed with lupus. It's scary. You're unsure of what is to come. Those are all natural feelings. I would like to offer a beginners guide to

November 7, 20200Comments

God is dope.

When doctors have told you your body is shutting down and my God says NOT TODAY, When you’ve spent months in a wheelchair and my God says no let’s walk,

by Rosadela Durruthy

Lupus Warrior Spotlight

October 24, 20200Comments

Lupus Warrior Spotlight – Kizzi Hogan

Kizza Hogan My Lupus Journey I suffered from many symptoms from an early age, around 10 years old. I was getting a "butterfly". rash on my face, struggled with being in the

October 24, 20200Comments

Lupus and Fatigue

When did you realize you were going to be tired everyday for the rest of your life? Even though I was diagnosed at age 23, I was still living a

by Rosadela Durruthy

Lupus Warrior Spotlight

October 23, 20200Comments

Lupus Warrior Spotlight – Emmitt Henderson

Emmitt Henderson, Ceo Male Lupus Warriors My name is Emmitt Henderson III, I was diagnosed with Systemic Lupus back in 1995, however, I had a visible rash all over my upper

by Rosadela Durruthy

Living With Lupus

October 9, 20201Comments

Supporting a loved one with lupus

Living with a chronic illness is hard. Living with an invisible chronic illness is harder. I can't count the amount of times I've had to suffer in silence because I

by Rosadela Durruthy

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